Canonical Allele Identifier: CA1190289607
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709932C= , CM000663.2:g.114709932C= GRCh38
NC_000001.10:g.115252553C= , CM000663.1:g.115252553C= GRCh37
NC_000001.9:g.115054076C= NCBI36
NG_007572.1:g.11963G= , LRG_92:g.11963G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-204G= MANE Select ENSP00000358548.4:n.291-204G=
ENST00000369535.4:c.291-204G= ENSP00000358548.4:n.291-204G=
NM_002524.4:c.291-204G= NP_002515.1:n.291-204G=
NM_002524.5:c.291-204G= MANE Select NP_002515.1:n.291-204G=